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Evaluation of the Patient-Reported Outcomes Measurement Information System in a Large Cohort of Patients With Inflammatory Bowel Diseases

机译:在大批炎症性肠病患者中评估患者报告的结果测量信息系统

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Background and Aims: Patient-reported outcomes (PROs) convey important aspects of health status, complementing physician-reported measures. The PRO Measurement Information System (PROMIS) provides valid, widely available measures applicable to patients with chronic illness and the general population. We sought to evaluate these measures in a large cohort of patients with inflammatory bowel disease (IBD). Methods: By using data from the Crohn's and Colitis Foundation Association Partners internet cohort, we performed cross-sectional and longitudinal analyses to evaluate associations between PROMIS measures and validated disease activity indices (Short Crohn's Disease Activity Index and Simple Clinical Colitis Activity Index) and the Short IBD Questionnaire quality-of-life instrument. Results: A total of 10,634 individuals (6689 with Crohn's disease and 3945 with ulcerative colitis or indeterminate colitis) completed PRO testing. Compared with the general population (mean PROMIS score, 50), IBD patients in this cohort reported more depression (mean, 54), anxiety (mean, 52), fatigue (mean, 56), sleep disturbance (mean, 52), and pain interference (mean, 53); and they had less social satisfaction (mean, 48). In each PROMIS domain, there was worse functioning with increasing levels of disease activity and worsening Short IBD Questionnaire scores (P < .001 for all). Longitudinal analyses showed improved PROMIS scores with improved disease activity and worsening PROMIS scores with worsening disease (P < .001 for all comparisons). Conclusions: In a cross-sectional and longitudinal study, we observed differences between patients with IBD and the general population in several important aspects of health. The improvement in diverse health outcome measures with improved disease control provides strong support for the construct validity of PROMIS measures in the IBD population. Their use should advance patient-centered outcomes research in IBD.
机译:背景和目的:患者报告的结局(PRO)传达了健康状况的重要方面,补充了医生报告的措施。 PRO度量信息系统(PROMIS)提供适用于慢性病患者和普通人群的有效且广泛可用的度量。我们试图在一大批炎症性肠病(IBD)患者中评估这些措施。方法:通过使用来自克罗恩氏和结肠炎基金会协会合作伙伴互联网队列的数据,我们进行了横断面和纵向分析,以评估PROMIS措施与已验证的疾病活动指数(克罗恩病活动指数和简单临床结肠炎活动指数)和简短的IBD问卷生活质量工具。结果:总共10,634人(6,689名克罗恩氏病和3945名溃疡性结肠炎或不确定性结肠炎)完成了PRO测试。与一般人群相比(平均PROMIS评分为50),该队列中的IBD患者报告的抑郁症(平均数为54),焦虑(平均数为52),疲劳(平均数为56),睡眠障碍(平均数为52)和疼痛干扰(平均53分);并且他们的社会满意度较低(平均48岁)。在每个PROMIS域中,随着疾病活动水平的提高和IBD短问卷调查评分的恶化,功能均变差(所有P均<.001)。纵向分析显示,改善的PROMIS评分具有改善的疾病活动性,而恶化的PROMIS评分则具有恶化的疾病(所有比较的P <0.001)。结论:在一项横断面和纵向研究中,我们观察到IBD患者与一般人群在健康的几个重要方面之间的差异。随着疾病控制的改善,各种健康结局指标的改进为IBD人群PROMIS指标的构建有效性提供了有力的支持。它们的使用应促进IBD中以患者为中心的结局研究。

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